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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 466562Erstellt: 24. Oktober 2026

Triethylamine → 3-[4-(3-Methylphenyl)-1-piperazinyl]-6-(methylsulfonyl)pyridazine

https://huagongshe.com/de/reaction/466562

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-(m-Tolyl)piperazineHCID 83111—
Edukt3-Chloro-6-(methylsulfonyl)pyridazineHCID 252476—
LösungsmittelBenzeneHCID 241—
Produkt3-[4-(3-Methylphenyl)-1-piperazinyl]-6-(methylsulfonyl)pyridazineHCID 1512460189%

Reaktionsschritte

A mixture of 3.2 parts of 3-chloro-6-(methylsulfonyl)pyridazine, 3 parts of 1-(3-methylphenyl)piperazine, 2 parts of N,N-diethylethanamine and 180 parts of benzene was stirred for 24 hours at reflux. The reaction mixture was evaporated. Water was added to the residue. The precipitated product was filtered off, washed with water and dissolved in trichloromethane. The solution was dried, filtered and evaporated. The residue was crystallized from methanol. The product was filtered off and dried, yielding 5 parts (89%) of 3-[4-(3-methylphenyl)-1-piperazinyl]-6-(methylsulfonyl)pyridazine; mp. 201° C. (compound 209).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05157035
Quelldatensatzuspto-grants-1992_10
ORD IDord-4747d6ab4c074086be6054a49c67d4fd
Quellennotizuspto-grants-1992_10